duratuss dm
Generic: dexbrompheniramine maleate, dextromethorphan hydrobromide and pseudoephedrine hydrochloride
Labeler: poly pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
duratuss dm
Generic Name
dexbrompheniramine maleate, dextromethorphan hydrobromide and pseudoephedrine hydrochloride
Labeler
poly pharmaceuticals, inc.
Dosage Form
LIQUID
Routes
Active Ingredients
dexbrompheniramine maleate 1 mg/5mL, dextromethorphan hydrobromide 10 mg/5mL, pseudoephedrine hydrochloride 30 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
50991-142
Product ID
50991-142_413a3951-d703-f14b-e063-6394a90a06dc
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2025-10-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
50991142
Hyphenated Format
50991-142
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
duratuss dm (source: ndc)
Generic Name
dexbrompheniramine maleate, dextromethorphan hydrobromide and pseudoephedrine hydrochloride (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/5mL
- 10 mg/5mL
- 30 mg/5mL
Packaging
- 473 mL in 1 BOTTLE (50991-142-16)
- 20 mL in 1 BOTTLE (50991-142-20)
Packages (2)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "413a3951-d703-f14b-e063-6394a90a06dc", "openfda": {"upc": ["0350991142167"], "unii": ["BPA9UT29BS", "9D2RTI9KYH", "6V9V2RYJ8N"], "rxcui": ["2727430"], "spl_set_id": ["413a3951-d704-f14b-e063-6394a90a06dc"], "manufacturer_name": ["Poly Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (50991-142-16)", "package_ndc": "50991-142-16", "marketing_start_date": "20251015"}, {"sample": false, "description": "20 mL in 1 BOTTLE (50991-142-20)", "package_ndc": "50991-142-20", "marketing_start_date": "20251015"}], "brand_name": "DURATUSS DM", "product_id": "50991-142_413a3951-d703-f14b-e063-6394a90a06dc", "dosage_form": "LIQUID", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "50991-142", "generic_name": "Dexbrompheniramine Maleate, Dextromethorphan Hydrobromide and Pseudoephedrine Hydrochloride", "labeler_name": "Poly Pharmaceuticals, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DURATUSS", "brand_name_suffix": "DM", "active_ingredients": [{"name": "DEXBROMPHENIRAMINE MALEATE", "strength": "1 mg/5mL"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/5mL"}, {"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "30 mg/5mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251015", "listing_expiration_date": "20261231"}